A potent proresolving mediator 17R-resolvin D2 from human macrophages, monocytes, and saliva DOI Creative Commons
Mélissa Simard, Robert Nshimiyimana, Nan Chiang

и другие.

Science Advances, Год журнала: 2024, Номер 10(47)

Опубликована: Ноя. 20, 2024

Production of specialized proresolving mediators (SPMs) during the resolution phase in acute inflammatory response is key to orchestrating complete resolution. Here, we uncovered a trihydroxy resolvin fresh human saliva. We identified and determined its stereochemistry as 7S,16R,17R-trihydroxy-4Z,8E,10Z,12E,14E,19Z-docosahexaenoic acid (17R-RvD2) using total organic synthesis matching physical properties. The 17R-RvD2 was produced by activated M2-like macrophages, M1-like peripheral blood monocytes. displayed potent functions (picomolar nanomolar). Topical application on mouse ear skin reduced neutrophilic infiltration (~50%). increased M2 markers CD206 CD163 monocyte–derived macrophages enhanced efferocytosis senescent red cells (EC 50 ~ 2.6 × 10 −14 M). In addition, RvD2 receptor equipotent epimer RvD2. also significantly phagocytosis Escherichia coli neutrophils. Together, these results establish previously unknown 17R-RvD2.

Язык: Английский

Diagnostic accuracy of bone marrow blood evaluation in Hemophagocytic Lymphohistiocytosis pediatric patients DOI

Elisa Caravaggi,

Federico Serana, Mattia Carini

и другие.

Annals of Clinical Biochemistry International Journal of Laboratory Medicine, Год журнала: 2024, Номер unknown

Опубликована: Окт. 17, 2024

Introduction Haemophagocytic lymphohistiocytosis (HLH) is a rare and serious immunological syndrome that involves strong activation of cytotoxic T lymphocytes macrophages. HLH determines cytokine-mediated tissue injury with contemporary multi-organ failure high fatality rate. Material methods A retrospective study was performed considering the medical records paediatric patients who underwent bone marrow aspirate for suspect HLH. The biomarkers evaluated were among those included in HLH-2004. Lactate dehydrogenase (LD) also evaluated. Haemophagocytosis blood smear slides. Results Enrolled 11 group 8 as controls. Haemoglobin fibrinogen resulted lower than controls, while triglycerides, serum ferritin LD increased. Blood triglycerides discriminated cases perfectly, sensitivity specificity 100%. Ferritin had 100% 83% (cut off ≥3,721 µg/L) 73% (the cut ≥1,903 U/L). found to have 75% ≤ 96 g/L). Total haemophagocytes cell counts not different between Only increased number phagocytized nucleated red cells (NRBC) be significantly patients. Erythrocytes phagocytosis (≥4/1,000 cells) only tended towards significance. Conclusions showed better diagnostic performance morphological evaluation. Among lineages engulfed by haemophagocytes, best obtained phagocytosed mature erythrocytes immature erythrocytes.

Язык: Английский

Процитировано

0

Increased calcification by erythrophagocytosis in aortic valvular interstitial cells DOI Creative Commons

Zihan Qin,

Magnus Bäck, Anders Franco‐Cereceda

и другие.

ESC Heart Failure, Год журнала: 2024, Номер unknown

Опубликована: Окт. 27, 2024

Abstract Background Calcific aortic valve disease (CAVD) progresses over time to severe stenosis and eventually heart failure. Recent evidence indicates that intraleaflet haemorrhage (ILH) strongly promotes CAVD progression. However, it remains poorly understood how mechanistically contributes valvular calcification. Method ILH was identified as iron deposition by morphological analysis. To elucidate the underlying mechanism, human interstitial cells (VIC) were cultured in presence of fresh or senescent red blood (RBC), simulating vivo conditions. Result common valves derived from patients with stenosis. VIC undergo erythrophagocytosis RBC, leading intracellular accumulation analogous observed following exposure extracellular iron. The RBC significantly intensified calcification, which mitigated ferroptosis inhibition. Conclusions Our results identify VIC, enhanced calcification through ferroptosis. This may be a crucial component pathophysiological mechanisms links accelerated

Язык: Английский

Процитировано

0

A potent proresolving mediator 17R-resolvin D2 from human macrophages, monocytes, and saliva DOI Creative Commons
Mélissa Simard, Robert Nshimiyimana, Nan Chiang

и другие.

Science Advances, Год журнала: 2024, Номер 10(47)

Опубликована: Ноя. 20, 2024

Production of specialized proresolving mediators (SPMs) during the resolution phase in acute inflammatory response is key to orchestrating complete resolution. Here, we uncovered a trihydroxy resolvin fresh human saliva. We identified and determined its stereochemistry as 7S,16R,17R-trihydroxy-4Z,8E,10Z,12E,14E,19Z-docosahexaenoic acid (17R-RvD2) using total organic synthesis matching physical properties. The 17R-RvD2 was produced by activated M2-like macrophages, M1-like peripheral blood monocytes. displayed potent functions (picomolar nanomolar). Topical application on mouse ear skin reduced neutrophilic infiltration (~50%). increased M2 markers CD206 CD163 monocyte–derived macrophages enhanced efferocytosis senescent red cells (EC 50 ~ 2.6 × 10 −14 M). In addition, RvD2 receptor equipotent epimer RvD2. also significantly phagocytosis Escherichia coli neutrophils. Together, these results establish previously unknown 17R-RvD2.

Язык: Английский

Процитировано

0